FDA recall record

SINUVA (mometasone furoate) sinus implant, 1350 mcg, 1 implant per pouch recall — FDA D-0167-2023

Failed Dissolution Specification; product did not meet the average 24-hour drug release rate (dissolution) specification stability time point at 9 months.

Class IIIclassification
D-0167-2023official record ID
Jan 25, 2023report date

Recall record at a glance

Official recordD-0167-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmIntersect ENT, Inc.
Report dateJan 25, 2023
Recall initiation dateJan 4, 2023
Quantity9898 pouches
LocationMenlo Park, CA, United States

Official product description

SINUVA (mometasone furoate) sinus implant, 1350 mcg, 1 implant per pouch, Rx Only, intersect ENT, 1555 Adams Drive, Menlo Park, CA 94025, NDC 10599-003-01.

Why the product was recalled

Failed Dissolution Specification; product did not meet the average 24-hour drug release rate (dissolution) specification stability time point at 9 months.

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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